Awards Nomination 20+ Million Readerbase
Indexed In
  • Open J Gate
  • Genamics JournalSeek
  • Academic Keys
  • JournalTOCs
  • ResearchBible
  • China National Knowledge Infrastructure (CNKI)
  • Scimago
  • Ulrich's Periodicals Directory
  • Electronic Journals Library
  • RefSeek
  • Hamdard University
  • EBSCO A-Z
  • OCLC- WorldCat
  • SWB online catalog
  • Virtual Library of Biology (vifabio)
  • Publons
  • MIAR
  • Scientific Indexing Services (SIS)
  • Euro Pub
  • Google Scholar
Share This Page
Journal Flyer
Flyer image
Light-triggerable liposomes for enhanced endo/lysosomal escape and gene silencing in PC12 cells
17th International Conference and Exhibition on Nanomedicine and Nanotechnology in Healthcare
November 23-24, 2017 Melbourne, Australia

Wei Deng, Wenjie Chen and Ewa M Goldys

Macquarie University, Australia

Scientific Tracks Abstracts: J Nanomed Nanotechnol

Abstract:

Liposomes are an effective gene/drug delivery system, widely used in biomedical applications including gene therapy and chemotherapy. Here we designed a photo-responsive liposome (lipVP) loaded with a photosensitizer verteporfin (VP). This photosensitizer is clinically approved for photodynamic therapy (PDT). LipVP was employed as a DNA carrier for pituitary adenylyl cyclase-activating polypeptide (PACAP) receptor 1 (PAC1R) gene knockdown in PC12 cells. This has been done by incorporating PAC1R antisense oligonucleotides inside the lipVP cavity. Cells which have taken up the lipVP were exposed to light from a UV light source. As a result of this exposure, reactive oxygen species (ROS) were generated from VP, destabilizing the endo/lysosomal membranes and enhancing the liposomal release of antisense DNA into the cytoplasm. Endo/lysosomal escape of DNA was documented at different time points based on quantitative analysis of colocalization between fluorescently labeled DNA and endo/lysosomes. The released antisense oligonucleotides were found to silence PAC1R mRNA. The efficiency of this photo-induced gene silencing was demonstrated by a 74±5% decrease in PAC1R fluorescence intensity. Following the light-induced DNA transfer into cells, cell differentiation with exposure to two kinds of PACAP peptides was observed to determine the cell phenotypic change after PAC1R gene knockdown.

Biography :

Wei Deng has received her PhD degree in Chemistry with nanotechnology background at Macquarie University, Australia in 2012. She was rewarded a highly competitive fellowship (Discovery Early Career Research Award) from the Australian Research Council in 2012. She is currently a Research Fellow in the Centre of Excellence in Nanoscale Biophotonics, Macquarie University. Her research fields were mainly focused on biomedical applications of liposomes and polymer nanoparticles, in particular, light (or X-ray)-controlled drug/gene delivery systems in cancer treatments.
Email:wei.deng@mq.edu.au